Variants studied for Factor VII deficiency

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
25	23	70	17	8	136

Gene and significance breakdown #

Total genes and gene combinations: 2

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
F7	25	23	70	7	6	124
F10, F7	0	0	0	10	2	12

Submitter and significance breakdown #

Total submitters: 11

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Illumina Laboratory Services, Illumina	3	1	64	15	8	91
OMIM	21	0	0	0	0	21
NIHR Bioresource Rare Diseases, University of Cambridge	2	15	3	0	0	20
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre	2	2	3	2	0	9
Baylor Genetics	0	2	0	0	0	2
Centre for Mendelian Genomics, University Medical Centre Ljubljana	0	2	0	0	0	2
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine	0	1	0	0	0	1
Genomic Research Center, Shahid Beheshti University of Medical Sciences	0	1	0	0	0	1
Knight Diagnostic Laboratories, Oregon Health and Sciences University	1	0	0	0	0	1
UNC Molecular Genetics Laboratory, University of North Carolina at Chapel Hill	0	1	0	0	0	1
Molecular Genetics, Labor Dr. Heidrich & Kollegen MVZ GmbH	0	1	0	0	0	1

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